HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157638_55157639insA , CM000681.2:g.55157638_55157639insA | GRCh38 |
NC_000019.9:g.55669006_55669007insA , CM000681.1:g.55669006_55669007insA | GRCh37 |
NC_000019.8:g.60360818_60360819insA | NCBI36 |
NG_007866.2:g.5094_5095insT , LRG_432:g.5094_5095insT | |
NG_032759.1:g.14084_14085insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.-50_-49insT MANE Select | ENSP00000341838.5:n.-50_-49insT | |
ENST00000665070.1:c.-50_-49insT | ENSP00000499482.1:n.-50_-49insT | |
ENST00000344887.9:c.-50_-49insT | ENSP00000341838.5:n.-50_-49insT | |
ENST00000586446.1:n.94_95insT | ||
ENST00000587176.5:n.135_136insT | ||
ENST00000587871.1:c.571_572insT | ||
ENST00000590463.1:n.78_79insT | ||
NM_000363.4:c.-50_-49insT , LRG_432t1:c.-50_-49insT | NP_000354.4:n.-50_-49insT | |
NM_000363.5:c.-50_-49insT MANE Select | NP_000354.4:n.-50_-49insT |